Canonical Allele Identifier: PA137484
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45977
ClinVar RCV Id: RCV000039212 RCV000764919 RCV000882752 RCV001273560
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Arg1804Trp
CA137483
NM_022124.6:c.5410C>T